Materials include primary papers, Reviews, Education materials, case studies, newsletters, conference materials, websites, slide kits, posters, videos, sales aids. Documents created by Medical Writers for medical professionals is usually highly scientific but often those intended for patients and the general public will also be written in clear, simple terms with minimal scientific jargon. The scientific and medical information and the language used in these documents written by medical writers will be tailored to suit the target audience, this could be patients, medical sales representatives, doctors, nurses and healthcare professionals. The role of a medical writer is to write high-quality scientific copy for the wide range of materials that a medical communications agency produces. A medical communications agency is tasked by their clients who are usually large pharmaceutical, biotech, medical device, healthcare or clinical research organisations to develop communication strategies that will assist in the delivery of effective campaigns. Ability to work in teams.Medical Communications - Senior Medical WriterĪ medical writer is key member of the editorial team within a medical communications agency. Good experience in managing global, cross functional teams or simple global projects.Knowledge of and experience in global regulatory environment and processes (key regulatory bodies, key documents, approval processes, safety reporting requirements). Strong ability to prioritize and manage multiple demands and projects.Good knowledge of biostatistics principles. Good operational knowledge of clinical trial reporting.M.Pharm/M.Sc Good communication skills in english (written, verbal, presentations) 2 to 3 years of regulatory medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus in-depth knowledge of medical writing processes.Maintain audit, SOP and training compliance. Contribute to cross-functional communication to optimize feedback and input towards high quality documents.Ħ. Ensure compliance of documentation to internal company standards and external regulatory guidelines.ĥ. Contribute to planning of data analyses and presentation to be used in CSRs.Ĥ. Liaise with medical/clinical experts, statisticians, investigators in concept development when protocol is being developed and work in a collaborative fashion for global/CPOs.ģ. To perform Quality Control (QC) of different regulatory documents.Ģ. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.ġ. Where you’re given opportunities to explore the power of digital and data. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. That’s how many lives our products touch.
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